HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252738Generated: November 1, 2026
Benzenesulfonyl chloride → HCID 86620415, compound
https://huagongshe.com/reaction/252738
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Lithium bis(trimethylsilyl)amide | HCID 57426343 | — |
| Reactant | HCID 86244451 | HCID 86244451 | — |
| Catalyst | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86620415 | HCID 86620415 | — |
Reaction Steps
Lithium hexamethyldisilazane (1M solution in THF; 0.81 mL) was added to a mixture of N-[5-(5-amino-6-chloropyridazin-3-yl)-4-methyl-1,3-thiazol-2-yl]acetamide (77 mg) and THF (1.3 mL) that had been cooled to 0° C. The reaction mixture was allowed to warm and was stirred at room temperature for 30 minutes. Benzenesulfonyl chloride (0.069 mL) was added and the reaction mixture was stirred at room temperature for 2 hours. Water (2 drops) was added to the reaction mixture. The mixture was evaporated and the residual solid was purified by preparative HPLC. The material so obtained was purified further by column chromatography on silica using a solvent gradient of 0% to 20% methanol in dichloromethane as eluent. There was thus obtained the title compound as a solid (2.5 mg); 1H NMR Spectrum: (DMSOd6) 2.15 (s, 3H), 2.40 (s, 3H), 7.05 (s, 1H), 7.45 (m, 3H), 7.80 (m, 2H); Mass Spectrum: M+H+ 424.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07868188B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-e17a838fe86944ac96de3f340fb579c0 |
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| Source note | uspto-grants-2011_01 |
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